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Consensus Rules in Variant Detection from Next-Generation Sequencing Data

A critical step in detecting variants from next-generation sequencing data is post hoc filtering of putative variants called or predicted by computational tools. Here, we highlight four critical parameters that could enhance the accuracy of called single nucleotide variants and insertions/deletions:...

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Détails bibliographiques
Auteurs principaux: Jia, Peilin, Li, Fei, Xia, Jufeng, Chen, Haiquan, Ji, Hongbin, Pao, William, Zhao, Zhongming
Format: Artigo
Langue:Inglês
Publié: Public Library of Science 2012
Sujets:
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC3371040/
https://ncbi.nlm.nih.gov/pubmed/22715385
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0038470
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